-
1
-
-
34347388866
-
-
Robinson, J.R. Introduction: Semi-solid formulations for oral drug delivery. Bulletin Technique Gattefossé, 1996, 11-13.
-
Robinson, J.R. Introduction: Semi-solid formulations for oral drug delivery. Bulletin Technique Gattefossé, 1996, 11-13.
-
-
-
-
2
-
-
1242337285
-
Solubilizing excipients in oral and injectable formulations
-
Strickley, R.G. Solubilizing excipients in oral and injectable formulations. Pharm. Res. 2004, 21 (2), 201-230.
-
(2004)
Pharm. Res
, vol.21
, Issue.2
, pp. 201-230
-
-
Strickley, R.G.1
-
3
-
-
0342617694
-
Lipid based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone, A.J.; Charman, W.N. Lipid based vehicles for the oral delivery of poorly water soluble drugs. Adv. Drug Deliv. Rev. 1997, 25, 103-128.
-
(1997)
Adv. Drug Deliv. Rev
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
4
-
-
0033812424
-
Lipids, lipophilic drugs, and oral drug delivery - Some emerging concepts
-
Charman, W. Lipids, lipophilic drugs, and oral drug delivery - Some emerging concepts. J. Pharm. Sci. 2000, 89 (8), 967-978.
-
(2000)
J. Pharm. Sci
, vol.89
, Issue.8
, pp. 967-978
-
-
Charman, W.1
-
5
-
-
0002361450
-
Key issues when formulating hydrophobic drugs with lipids
-
Pouton, C.W. Key issues when formulating hydrophobic drugs with lipids. Bulletin Technique Gattefossé 1999, 41-49.
-
(1999)
Bulletin Technique Gattefossé
, pp. 41-49
-
-
Pouton, C.W.1
-
6
-
-
0033805858
-
-
Pouton, C.W. Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying, and self-microemulsifying drug delivery systems. Eur. J. Pharm. Sci. 2000, 11 (Suppl. 2), S93-S98.
-
Pouton, C.W. Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying, and "self-microemulsifying" drug delivery systems. Eur. J. Pharm. Sci. 2000, 11 (Suppl. 2), S93-S98.
-
-
-
-
7
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik, T.; Benita, S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Europ. J. Pharm. Biopharm. 2000, 50, 179-188.
-
(2000)
Europ. J. Pharm. Biopharm
, vol.50
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
8
-
-
1842684453
-
Self-emulsifying drug delivery sytems (SEDDS) for improved oral delivery of lipophilic drugs
-
Gursoy, R.N.; Benita, S. Self-emulsifying drug delivery sytems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother. 2004, 58, 173-182.
-
(2004)
Biomed Pharmacother
, vol.58
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
9
-
-
0034614208
-
Microemulsion based media as novel drug delivery systems
-
Lawrence M.J.; Rees, G.D. Microemulsion based media as novel drug delivery systems. Adv. Drug Deliv. Rev. 2000, 45, 89-121.
-
(2000)
Adv. Drug Deliv. Rev
, vol.45
, pp. 89-121
-
-
Lawrence, M.J.1
Rees, G.D.2
-
10
-
-
4344578729
-
Susceptibility to lipase mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid based microemulsion formulation
-
Porter, C.J.H.; Kaukonen, A.M.; Boyd, B.J.; Edwards, G.A.; Charman, W. Susceptibility to lipase mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid based microemulsion formulation. Pharm. Res. 2004, 21 (8), 1405-1412.
-
(2004)
Pharm. Res
, vol.21
, Issue.8
, pp. 1405-1412
-
-
Porter, C.J.H.1
Kaukonen, A.M.2
Boyd, B.J.3
Edwards, G.A.4
Charman, W.5
-
11
-
-
34347400236
-
Formulation of poorly water-soluble drugs for oral administration
-
Pouton, C.W. Formulation of poorly water-soluble drugs for oral administration. Bulletin Technique Gattefossé 2005, 39-51.
-
(2005)
Bulletin Technique Gattefossé
, pp. 39-51
-
-
Pouton, C.W.1
-
12
-
-
33646287079
-
Gastrointestinal absorption of peptides using microemulsions as delivery systems
-
Ritschel, W.A. Gastrointestinal absorption of peptides using microemulsions as delivery systems. Bulletin Technique Gattefossé, 1990, 7-22.
-
(1990)
Bulletin Technique Gattefossé
, pp. 7-22
-
-
Ritschel, W.A.1
-
13
-
-
0347022226
-
Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: Contribution of emulsification versus digestibility
-
De Smidt, P.C., Campanero, M.A. Trocóniz, I.F. Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: contribution of emulsification versus digestibility. Int. J. Pharm. 2004, 270, 109-118.
-
(2004)
Int. J. Pharm
, vol.270
, pp. 109-118
-
-
De Smidt, P.C.1
Campanero, M.A.2
Trocóniz, I.F.3
-
14
-
-
0343051926
-
Influence of lipolysis on drug absorption from the gastro intestinal tract
-
MacGregor, K.J.; Embleton, J.K., Lacy, J.E.; Perry, E.A.; Solomon, L.J.; Seager, H.; Pouton, C.W. Influence of lipolysis on drug absorption from the gastro intestinal tract. Adv. Drug Deliv. Rev. 1997, 25, 33-46.
-
(1997)
Adv. Drug Deliv. Rev
, vol.25
, pp. 33-46
-
-
MacGregor, K.J.1
Embleton, J.K.2
Lacy, J.E.3
Perry, E.A.4
Solomon, L.J.5
Seager, H.6
Pouton, C.W.7
-
15
-
-
0035478113
-
From the interaction of lipid vesicles with intestinal epithelial cell membranes to the formation and secretion of chylomicrons
-
Shen, H.; Howles, P.; Tso, P. From the interaction of lipid vesicles with intestinal epithelial cell membranes to the formation and secretion of chylomicrons. Adv. Drug Deliv. Rev. 2001, 50, S103-S125.
-
(2001)
Adv. Drug Deliv. Rev
, vol.50
-
-
Shen, H.1
Howles, P.2
Tso, P.3
-
16
-
-
0035984949
-
Lipid-based formulations for intestinal lymphatic delivery
-
O'Driscoll, C.M. Lipid-based formulations for intestinal lymphatic delivery. Eur. J. Pharm. Sci. 2002, 15, 405-415.
-
(2002)
Eur. J. Pharm. Sci
, vol.15
, pp. 405-415
-
-
O'Driscoll, C.M.1
-
17
-
-
0030614844
-
Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH
-
Charman, W.N.; Porter, C.J.H.; Mithani, S.; Dressman, J. Physicochemical and physiological mechanisms for the effects of food on drug absorption: The role of lipids and pH. J. Pharm. Sci. 1997, 86 (3), 269-282.
-
(1997)
J. Pharm. Sci
, vol.86
, Issue.3
, pp. 269-282
-
-
Charman, W.N.1
Porter, C.J.H.2
Mithani, S.3
Dressman, J.4
-
18
-
-
0014273339
-
Control of gastric emptying
-
Hunt, J.N.; Knox, M.T. Control of gastric emptying. Am. J. Dig. Dis. 1968, 13, 372-375.
-
(1968)
Am. J. Dig. Dis
, vol.13
, pp. 372-375
-
-
Hunt, J.N.1
Knox, M.T.2
-
19
-
-
0014253851
-
A relation between the chain length of fatty acids and and the slowing of gastric emptying
-
Hunt, J.N.; Knox, M.T. A relation between the chain length of fatty acids and and the slowing of gastric emptying. J. Physiol. (London), 1968, 194, 327-336.
-
(1968)
J. Physiol. (London)
, vol.194
, pp. 327-336
-
-
Hunt, J.N.1
Knox, M.T.2
-
20
-
-
0035189031
-
Lipid-based formulations for oral administration: Opportunities for bioavailability enhancement and lipoprotein targeting of lipophilic drugs
-
Porter, Ch.; Charman, N. Lipid-based formulations for oral administration: opportunities for bioavailability enhancement and lipoprotein targeting of lipophilic drugs. J. Recept. Signal Transduct. Rese. 2001, 21 (2&3) 215-257.
-
(2001)
J. Recept. Signal Transduct. Rese
, vol.21
, Issue.2-3
, pp. 215-257
-
-
Porter, C.1
Charman, N.2
-
21
-
-
0035290059
-
Active secretion and enterocytic drug metabolism barriers to drug absorption
-
Wacher, V.J.; Salphati, L.;Benet, L.Z. Active secretion and enterocytic drug metabolism barriers to drug absorption. Adv. Drug. Del. Rev. 2001, 46, 89-102.
-
(2001)
Adv. Drug. Del. Rev
, vol.46
, pp. 89-102
-
-
Wacher, V.J.1
Salphati, L.2
Benet, L.Z.3
-
22
-
-
0344012523
-
Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with Improved oral bioavailability
-
Gao, P.; Rush, B.D.; Pfund, W.P.; Huang, T.; Bauer, J.M.; Morozowich, W.; Kuo, M.S.; Hageman, M.J. Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with Improved oral bioavailability. J. Pharm. Sci. 2003, 92 (12), 2386-2398.
-
(2003)
J. Pharm. Sci
, vol.92
, Issue.12
, pp. 2386-2398
-
-
Gao, P.1
Rush, B.D.2
Pfund, W.P.3
Huang, T.4
Bauer, J.M.5
Morozowich, W.6
Kuo, M.S.7
Hageman, M.J.8
-
23
-
-
0002647156
-
Digestible emulsions and microemulsions for optimum oral delivery of hydrophobic drugs
-
Hutchinson, K. Digestible emulsions and microemulsions for optimum oral delivery of hydrophobic drugs. Bulletin Technique Gattefossé, 1994, 67-74.
-
(1994)
Bulletin Technique Gattefossé
, pp. 67-74
-
-
Hutchinson, K.1
-
24
-
-
0037407282
-
Human jejunal permeability of cyclosporine A: Influence of surfactants on P-glycoprotein efflux in Caco 2 cells
-
Chiu, Y.Y.; Higaki, K.; Neudeck, B.L.; Barnett, J.L.; Welage, L.S.; Amidon, G.L. Human jejunal permeability of cyclosporine A: Influence of surfactants on P-glycoprotein efflux in Caco 2 cells. Pharm. Res. 2003, 20 (5), 749-756.
-
(2003)
Pharm. Res
, vol.20
, Issue.5
, pp. 749-756
-
-
Chiu, Y.Y.1
Higaki, K.2
Neudeck, B.L.3
Barnett, J.L.4
Welage, L.S.5
Amidon, G.L.6
-
25
-
-
0033427847
-
Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability
-
Yu, L., Bridgers, A.; Polli, J.; Vickers, A.; Long, S.; Roy, A.; Winnike, R.; Coffin, M. Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability. Pharm. Res. 1999, 16 (12) 1812-1817.
-
(1999)
Pharm. Res
, vol.16
, Issue.12
, pp. 1812-1817
-
-
Yu, L.1
Bridgers, A.2
Polli, J.3
Vickers, A.4
Long, S.5
Roy, A.6
Winnike, R.7
Coffin, M.8
-
26
-
-
0031780652
-
Interaction of a self-emulsifying lipid delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge
-
Gershanik, T.; Benzeno, S.; Benita, S. Interaction of a self-emulsifying lipid delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge. Pharm. Res. 1998, 15 (6), 863-869.
-
(1998)
Pharm. Res
, vol.15
, Issue.6
, pp. 863-869
-
-
Gershanik, T.1
Benzeno, S.2
Benita, S.3
-
27
-
-
0033816196
-
Intestinal permeation enhancers
-
Aungst, B.J. Intestinal permeation enhancers. J. Pharm. Sci. 2000, 89 (4), 429-442.
-
(2000)
J. Pharm. Sci
, vol.89
, Issue.4
, pp. 429-442
-
-
Aungst, B.J.1
-
28
-
-
0033369169
-
The role of sorption promoters in increasing the bioavailability of drugs in oral preparations
-
Sharma, P.; Chawla, H.P.S.; Panchagnula, R.; The role of sorption promoters in increasing the bioavailability of drugs in oral preparations. Drugs Future 1999, 24 (11), 1221-1240.
-
(1999)
Drugs Future
, vol.24
, Issue.11
, pp. 1221-1240
-
-
Sharma, P.1
Chawla, H.P.S.2
Panchagnula, R.3
-
29
-
-
0038537242
-
The effect of pluronic block copolymers and cremophor EL on intestinal lipoprotein processing and the potential link with P-glykoprotein in Caco-2 cells
-
Seeballuck, F.; Ashford, M.B.; O'Driscoll, C.M. The effect of pluronic block copolymers and cremophor EL on intestinal lipoprotein processing and the potential link with P-glykoprotein in Caco-2 cells. Pharm. Res. 2003, 20 (7), 1085-1092.
-
(2003)
Pharm. Res
, vol.20
, Issue.7
, pp. 1085-1092
-
-
Seeballuck, F.1
Ashford, M.B.2
O'Driscoll, C.M.3
-
30
-
-
14144249452
-
Evaluation of chylomicron flow blocking approach to investigate the lymphatic transport of lipophilic drugs
-
Dahan, A.; Hoffmann, A. Evaluation of chylomicron flow blocking approach to investigate the lymphatic transport of lipophilic drugs. Eur. J. Pharm. Sci. 2005, 24, 381-388.
-
(2005)
Eur. J. Pharm. Sci
, vol.24
, pp. 381-388
-
-
Dahan, A.1
Hoffmann, A.2
-
31
-
-
0035478436
-
In vitro assessment of oral lipid based formulations
-
Porter, C.J.H.; Charman, W.N. In vitro assessment of oral lipid based formulations. Adv. Drug Deliv. Rev. 2001, 50, S127-S147.
-
(2001)
Adv. Drug Deliv. Rev
, vol.50
-
-
Porter, C.J.H.1
Charman, W.N.2
-
32
-
-
0036080082
-
Multivariate methods in pharmaceutical applications
-
Gabrielsson, J.; Lindberg, N.O.; Lundstedt, T. Multivariate methods in pharmaceutical applications. J. Chemometr. 2002, 16, 141-160.
-
(2002)
J. Chemometr
, vol.16
, pp. 141-160
-
-
Gabrielsson, J.1
Lindberg, N.O.2
Lundstedt, T.3
-
33
-
-
0344629793
-
Multivariate methods in the development of a new tablet formulation
-
Gabrielsson, J.; Lindberg, N.O.; Pålsson, M.; Nickolasson, F.; Sjöström, M.; Lundstedt, T. Multivariate methods in the development of a new tablet formulation. Drug. Dev. Ind. Pharm. 2003, 29 (10) 1053-1075.
-
(2003)
Drug. Dev. Ind. Pharm
, vol.29
, Issue.10
, pp. 1053-1075
-
-
Gabrielsson, J.1
Lindberg, N.O.2
Pålsson, M.3
Nickolasson, F.4
Sjöström, M.5
Lundstedt, T.6
-
34
-
-
0344514705
-
Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine
-
Odeberg, J.M.; Kaufmann, P.; Kroon, K.G.; Höglund, P. Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine. Eur. J. Pharm. Sci. 2003, 20, 375-382.
-
(2003)
Eur. J. Pharm. Sci
, vol.20
, pp. 375-382
-
-
Odeberg, J.M.1
Kaufmann, P.2
Kroon, K.G.3
Höglund, P.4
-
35
-
-
0003826721
-
-
Umetics AB: Sweden
-
Erikksson, L; Johansson, E; Kettaneh-Wold, and Wold, S. Multi- and Megavariate Data Analysis. Principles and Applications; Umetics AB: Sweden, 2001, 71-77.
-
(2001)
Multi- and Megavariate Data Analysis. Principles and Applications
, pp. 71-77
-
-
Erikksson, L.1
Johansson, E.2
Kettaneh-Wold3
Wold, S.4
-
37
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Huberstone, A.J.; Charman, W.N., Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv. Drug Delive. Rev. 1997, 25, 103-128.
-
(1997)
Adv. Drug Delive. Rev
, vol.25
, pp. 103-128
-
-
Huberstone, A.J.1
Charman, W.N.2
-
38
-
-
25444464372
-
Bioavailability of seocalcitol I. Relating solubility in biorelevant media with oral bioavailability in rats - Effect of medium and long chain triglycerides
-
Grove, M; Pedersen, G.P.; Nielsen, J.L.; Müllertz, A., Bioavailability of seocalcitol I. Relating solubility in biorelevant media with oral bioavailability in rats - Effect of medium and long chain triglycerides. J. Pharm. Sci. 2005, 94 (8), 1830-1838.
-
(2005)
J. Pharm. Sci
, vol.94
, Issue.8
, pp. 1830-1838
-
-
Grove, M.1
Pedersen, G.P.2
Nielsen, J.L.3
Müllertz, A.4
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